Sentinel Lymph Node Biopsy vs No Axillary Surgery in Patients With Small Breast Cancer and Negative Results on Ultrasonography of Axillary Lymph Nodes

医学 前哨淋巴结 乳腺癌 随机对照试验 腋窝 腋窝淋巴结 哨兵节点 活检 外科 累积发病率 乳房外科 保乳手术 放射科 乳房切除术 癌症 内科学 移植
作者
Oreste ­Gentilini,Edoardo Botteri,Claudia Sangalli,Viviana Galimberti,Mauro Porpiglia,Roberto Agresti,Alberto Luini,Giuseppe Viale,Enrico Cassano,Nickolas Peradze,Antonio Toesca,Giulia Massari,Virgilio Sacchini,Elisabetta Munzone,Maria Cristina Leonardi,Francesca Cattadori,Rosa Di Micco,Emanuela Esposito,Adele Sgarella,Silvia Cattaneo,Massimo Busani,Massimo Dessena,Anna Bianchi,Elisabetta Cretella,Francisco Ripoll Orts,Michael D. Mueller,Corrado Tinterri,Badir Jorge Chahuan Manzur,Chiara Benedetto,Paolo Veronesi,Fabio Bassi,Fulvio Borella,Pietro Caldarella,Marco Colleoni,Giovanni Corso,Silvia Dellapasqua,Alberta Ferrari,Carlos A. Garcia‐Etienne,Damiano Gentile,Alessandro Germano,L.P. Grosso,Mattia Intra,Monica Iorfida,José Vila,Gennaro Limite,Germana Lissidini,G Macellari,Francesca Magnoni,Ilaria Maugeri,Manuelita Mazza,Emilia Montagna,Paola Naninato,Luca Nicosia,Roberto Orecchia,Alberto F. Pierini,Claudia Rauh,Massimo Rinaldo,Anna Rotili,Nicole Rotmensz,Anna Rita Vento,Veronica Zuber
出处
期刊:JAMA Oncology [American Medical Association]
卷期号:9 (11): 1557-1557 被引量:126
标识
DOI:10.1001/jamaoncol.2023.3759
摘要

Importance Sentinel lymph node biopsy (SLNB) is the standard of care for axillary node staging of patients with early breast cancer (BC), but its necessity can be questioned since surgery for examination of axillary nodes is not performed with curative intent. Objective To determine whether the omission of axillary surgery is noninferior to SLNB in patients with small BC and a negative result on preoperative axillary lymph node ultrasonography. Design, Setting, and Participants The SOUND (Sentinel Node vs Observation After Axillary Ultra-Sound) trial was a prospective noninferiority phase 3 randomized clinical trial conducted in Italy, Switzerland, Spain, and Chile. A total of 1463 women of any age with BC up to 2 cm and a negative preoperative axillary ultrasonography result were enrolled and randomized between February 6, 2012, and June 30, 2017. Of those, 1405 were included in the intention-to-treat analysis. Data were analyzed from October 10, 2022, to January 13, 2023. Intervention Eligible patients were randomized on a 1:1 ratio to receive SLNB (SLNB group) or no axillary surgery (no axillary surgery group). Main Outcomes and Measures The primary end point of the study was distant disease–free survival (DDFS) at 5 years, analyzed as intention to treat. Secondary end points were the cumulative incidence of distant recurrences, the cumulative incidence of axillary recurrences, DFS, overall survival (OS), and the adjuvant treatment recommendations. Results Among 1405 women (median [IQR] age, 60 [52-68] years) included in the intention-to-treat analysis, 708 were randomized to the SLNB group, and 697 were randomized to the no axillary surgery group. Overall, the median (IQR) tumor size was 1.1 (0.8-1.5) cm, and 1234 patients (87.8%) had estrogen receptor–positive ERBB2 (formerly HER2 or HER2/neu ), nonoverexpressing BC. In the SLNB group, 97 patients (13.7%) had positive axillary nodes. The median (IQR) follow-up for disease assessment was 5.7 (5.0-6.8) years in the SLNB group and 5.7 (5.0-6.6) years in the no axillary surgery group. Five-year distant DDFS was 97.7% in the SLNB group and 98.0% in the no axillary surgery group (log-rank P = .67; hazard ratio, 0.84; 90% CI, 0.45-1.54; noninferiority P = .02). A total of 12 (1.7%) locoregional relapses, 13 (1.8%) distant metastases, and 21 (3.0%) deaths were observed in the SLNB group, and 11 (1.6%) locoregional relapses, 14 (2.0%) distant metastases, and 18 (2.6%) deaths were observed in the no axillary surgery group. Conclusions and Relevance In this randomized clinical trial, omission of axillary surgery was noninferior to SLNB in patients with small BC and a negative result on ultrasonography of the axillary lymph nodes. These results suggest that patients with these features can be safely spared any axillary surgery whenever the lack of pathological information does not affect the postoperative treatment plan. Trial Registration ClinicalTrials.gov Identifier: NCT02167490
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